A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544028



Internal ID20917269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33651403..33651677hg38UCSC Ensembl
chr3:33692895..33693169hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262064
Samples
Known GenesCLASP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544028
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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